Aminopyridine derivatives having aurora a selective inhibitory action

a technology of aminopyridine and selective inhibitory action, which is applied in the field of new drugs, can solve the problems of difficult development of subtype-selective drugs, and no report on an aminopyridine derivative having an excellent aurora selective inhibitory action, and achieve the effect of improving the activity of natural killer cells

Active Publication Date: 2012-01-24
MSD KK
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Meanwhile, with regard to the Aurora kinase inhibitor, development of subtype-selective drugs has been thought to be difficult in view of high homology among subtypes, protein structure analysis and the like; and although there have been known reports on drugs such as ZM447439 which inhibit both Aurora A and Aurora B at the same time [J.
However, there has been no report on an aminopyridine derivative having an excellent Aurora A selective inhibitory action thus far.

Method used

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  • Aminopyridine derivatives having aurora a selective inhibitory action
  • Aminopyridine derivatives having aurora a selective inhibitory action
  • Aminopyridine derivatives having aurora a selective inhibitory action

Examples

Experimental program
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Effect test

working examples

[0420]In a thin-layer chromatography of Examples and Referential Examples, Silica gel60F254 (Merck) was used as a plate and a UV detector was used in a detecting method. As silica gel for the column, Wakogel™ C-300 or C-200 (Wako Pure Chemical) or NH (FUJI SILYSIA CHEMICAL) was used. In a reversed phase preparative liquid chromatography, CombiPrep Pro C18 (YMC) was used as a column and a 0.1% aqueous trifluoroacetic acid solution and a 0.1% solution of trifluoroacetic acid in acetonitrile were used in a mobile phase. MS spectra were measured using JMS-SX102A (JEOL) or QUATTROII (Micro Mass). NMR spectra were measured using a spectrometer in a type of Gemini-200 (200 MHz; Varian), Gemini-300 (300 MHz; Varian), VXR-300 (300 MHz; Varian), Mercury 400 (400 MHz; Varian) or Inova 400 (400 MHz; Varian) and all 8 values are represented in ppm.

[0421]Meanings of abbreviations used in the NMR measurement are as follows.[0422]s: singlet[0423]d: doublet[0424]dd: double doublet[0425]t: triplet[04...

example 1

Synthesis of 2-(((1S,4S)-5-(3-chloro-2-fluorobenzoyl)-2,5-diazabicyclo[2.2.1]hept-2-yl)methyl)-6-methyl-N-1H-pyrazol-3-ylpyrimidine-4-amine

(1) Synthesis of N-(1-tert-butyl-1H-pyrazol-5-yl)-2-chloro-6-methylpyrimidine-4-amine

[0440]

[0441]A mixture of 9.70 g of 2,4-dichloro-6-methyl-pyrimidine, 4.50 g of 1-tert-butyl-1H -pyrazol-5-amine obtained in Reference Example 1, 1.79 g of 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene, 1.60 g of tris(dibenzylideneacetone)dipalladium(0)-chloroform complex, 13.27 g of potassium phosphate, and 100 ml of 1,4-dioxane was stirred at 100° C. for 12 hours, cooled to room temperature, and then diluted with ethyl acetate. An insoluble matter was filtered off using Celite and the resulting ethyl acetate solution was washed with water and saturated brine. The organic layer was dried over anhydrous magnesium sulfate and filtered, and the filtrate was concentrated. The residue was purified by a silica gel column chromatography (eluent: hexane / ethyl acetate=9...

example 2

Synthesis of 2-(((1S,4S)-5-(2-fluoro-3-(trifluoromethyl)benzoyl)-2,5-diazabicyclo[2.2.1]hept-2-yl)methyl)-6-methyl-N-1H-pyrazol-3-ylpyrimidine-4-amine

[0454]1H-NMR (CDCl3) δ: 8.45-8.00 (br, 1H), 7.72-7.61 (m, 2H), 7.51 (dd, J=7.3, 2.4 Hz, 1H), 7.32 (t, J=8.0 Hz, 1H), 6.87 (s, 1H), 6.28 and 6.21 (each d, J=2.4 Hz, total 1H), 4.94-2.80 (m, 8H), 2.41-2.36 (m, 3H), 2.15-2.04 (m, 1H), 1.90-1.80 (m, 1H).

[0455]Mass: 476 (M+1)+.

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Abstract

The present invention relates to a compound of general formula I:wherein:n1 and n2 are the same or different, and are 0 or 1; R is aryl, heteroaryl, etc.; Re is hydrogen atom or lower alkyl; two groups selected from four groups consisting of (i) either one of Ra1 and Ra1′, (ii) either one of Ra2 and Ra2′, (iii) either one of Rb1 and Rb1′, and (iv) either one of Rb2 and Rb2′, are combined to form —(CH2)n— where n is 1, 2 or 3; and among Ra1, Ra1′, Ra2, Ra2′, Rb1, Rb1′, Rb2 and Rb2′, the groups which do not form —(CH2)n— are each independently hydrogen atom, etc.; X1, X2, X3 and X4 are each independently CH, N, etc.; Y1, Y2, Y3 and Y4 are the same or different and are CH or N, etc.; W is a 5-membered aromatic heterocyclic group,or a pharmaceutically acceptable salt or ester thereof.

Description

PRIORITY CLAIM[0001]This application is a §371 application of PCT / JP2007 / 059413 that was filed on Apr. 25, 2007, which claims priority from Japanese Application No. 2006-124475, filed on Apr. 27, 2006, now expired.TECHNICAL FIELD[0002]The present invention relates to novel aminopyridine derivatives which are useful in the pharmaceutical field, and more particularly, to those which inhibit the growth of tumor cells based on an Aurora A selective inhibitory action and exhibit an antitumor effect, and also to an Aurora A selective inhibitor and an antitumor agent containing them.BACKGROUND ART[0003]Aurora kinase is a serine / threonine kinase involved in cell division. With regard to the Aurora kinase, three subtypes of A, B and C are known at present, and they have very high homology to each other. Aurora A participates in the maturation and distribution of centrosome or in the formation of spindle body. On the other hand, it is believed that Aurora B participates in the aggregation and...

Claims

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Application Information

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Patent Type & AuthorityPatents(United States)
IPC IPC(8): C07D239/42C07D239/02C07D403/14
CPCC07D487/08A61P35/00A61P43/00
InventorKATO, TETSUYAKAWANISHI, NOBUHIKOMITA, TAKASHINAGAI, KEITANONOSHITA, KATSUMASAOHKUBO, MITSURU
OwnerMSD KK